溶瘤病毒
癌症研究
细胞
肽
溶解
多重耐药
体内
细胞膜
材料科学
化学
肿瘤细胞
生物
抗药性
生物化学
微生物学
生物技术
作者
Jia Yang,Rui Zheng,Muhetaerjiang Mamuti,Da‐Yong Hou,Yongdan Zhao,Hong‐Wei An,Hao Wang,Yuliang Zhao
出处
期刊:Biomaterials
[Elsevier]
日期:2022-03-29
卷期号:284: 121488-121488
被引量:11
标识
DOI:10.1016/j.biomaterials.2022.121488
摘要
Due to intrinsic and acquired chemo/radiotherapy-resistance, renal cell carcinoma shows limited therapeutic response to clinically utilized targeting drugs. Here a tumor-activated oncolytic peptide nanomachine is devised to selectively lysing tumor cell membrane without causing drug resistance. Specifically, in the acidic tumor microenvironment, the oncolytic peptide nanomachine automatically activated through morphologically transformation from nanoparticles to nanofibrils with restoring α-helical conformation, which physically bind to tumor cell membrane with multiple (spatially correlated and time-resolved) interactions and subsequently lyse local cell membrane. The IC50 of the oncolytic peptide nanomachine is as low as 2.44 μM and it inhibit up to 90% of tumor cells within 2 h with unique bystander killing effect. In vivo, the tumor inhibition rate of the oncolytic peptide nanomachine is 71% without off-target activity and hemolytic activity. These results support that tumor-selective oncolytic peptide nanomachine represent a promising alternative approach for multidrug-resistant tumor treatments by inducing cell membrane lysis.
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